A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132996



Internal ID20700036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82651420..82653222hg38UCSC Ensembl
chr5:81947239..81949041hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg381803
hg191803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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